Severe Dejerine-Sottas disease with respiratory failure and dysmorphic features in association with a PMP22 point mutation and a 3q23 microdeletion. (2012)

First Author: Voermans NC


No abstract provided

Bibliographic Information

Digital Object Identifier:

PubMed Identifier: 22734911

Publication URI:

Type: Journal Article/Review

Volume: 17

Parent Publication: Journal of the peripheral nervous system : JPNS

Issue: 2

ISSN: 1085-9489